The Medela Thopaz+ Chest Drainage System represents a breakthrough in thoracic post-operative care. Designed for use after thoracic and cardiac surgery or spontaneous pneumothorax, the Thopaz+ provides precise, controlled chest drainage with continuous digital monitoring—replacing outdated wall-suction systems with an intelligent, mobile solution.
Thopaz+ delivers regulated negative pressure near the patient’s chest, maintaining consistent vacuum levels even with patient movement. It uses digital airflow and pressure monitoring to ensure optimal drainage while reducing complications and enabling earlier, evidence-based decisions for chest tube removal.
Key Features and Benefits
Digital Precision: Real-time data tracking for both air leak (ml/min) and fluid output (ml/h), offering clinicians a reliable and objective basis for decision-making.
Regulated Suction at Source: Automatically maintains prescribed negative pressure directly at the patient's chest, ensuring safe and effective drainage without dependence on wall suction.
Enhanced Patient Mobility: Compact and lightweight, Thopaz+ supports early patient mobilization—reducing risks of pulmonary complications and promoting faster recovery.
Visual and Audible Alarms: Smart alarms notify healthcare providers of occlusions, high fluid output, low battery, or pressure deviations, ensuring patient safety at all times.
Data Recording and Transfer: Integrated memory stores up to 10 days of treatment data, which can be exported for analysis or documentation—improving care continuity and supporting hospital quality initiatives.
Quiet and User-Friendly: Operates with minimal noise and features an intuitive touchscreen interface, enabling easy setup and monitoring by staff.
Cost-Effective and Proven: Clinical studies show that Thopaz+ can significantly reduce hospital stay lengths and chest tube duration, lowering overall care costs and improving throughput.
Clinical Applications
Thoracic surgery (e.g., lobectomy, pneumonectomy)
Cardiac surgery (e.g., CABG, valve repair)
Spontaneous or traumatic pneumothorax
Pleural effusion management
Post-operative air leak monitoring
Why Choose Thopaz+?
The Thopaz+ system reflects a new standard in post-surgical chest drainage care—combining safety, portability, and clinical accuracy in a system backed by robust evidence and worldwide adoption across top hospitals. Its ability to standardize care while improving patient comfort makes it the go-to choice for modern thoracic and cardiac units.
Specifications
General Specifications
Device Type: Digital, portable chest drainage and monitoring system
Intended Use: Post-operative drainage of the pleural or mediastinal space, spontaneous/traumatic pneumothorax, and air/fluid evacuation in thoracic and cardiac patients
Suction and Pressure Regulation
Suction Range:
Adjustable from -5 to -40 cmH₂O
Vacuum Regulation:
Actively regulated at the patient’s chest (not dependent on wall suction)
Suction Modes:
Regulated (continuous) or Off (gravity drainage)
Drainage Monitoring
Air Leak Monitoring:
Digital, continuous display in ml/min
Fluid Drainage Monitoring:
Volume tracked in ml/h and total volume (up to 2000 ml)
Real-Time Feedback:
Graphical and numerical display of trends and events
Monitoring Duration:
Up to 10 days of storage in internal memory
User Interface
Display Type:
High-resolution, color touchscreen (intuitive icons and visual alarms)
Alarm System:
Visual and audible alarms for:
High output
Occlusion
Low battery
Leak/pressure deviation
Canister full
Power and Battery
Battery Type:
Rechargeable lithium-ion battery
Battery Life:
Up to 12 hours of operation per charge
Charging Time:
Approx. 2.5–3 hours to full charge
Power Supply:
100–240V AC / 50–60 Hz
Canister and Tubing
Canister Capacity:
Disposable canister: 300 ml, 800 ml, or 2,000 ml
Tubing Sets:
Single-use, sterile sets available for various surgical applications
Integrated Hydrophobic Filter:
Protects device and environment from aerosol contamination
Data Management
Data Storage:
Up to 10 days of continuous therapy data
Data Export:
Via USB for analysis, quality control, or electronic medical records (EMR) integration
Physical Dimensions
Device Dimensions (W x H x D):
Approx. 220 × 180 × 120 mm
Weight (without canister):
Approx. 2.0–2.3 kg (4.4–5 lbs)
Certifications and Compliance
Medical Standards:
CE-marked (per EU MDR)
FDA-cleared (U.S. market)
ISO 13485 certified
Ingress Protection:
IP22 (protected against dripping water when tilted up to 15°)